
Sr. Specialist, Medical Affairs
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
ESSENTIAL DUTIES and RESPONSIBILITIES
- Serve as the medical/ clinical subject matter expert to both internal and external customers for sustaining and some product development efforts.
- Develops and delivers medical/clinical input into relevant medical device technical documents (e.g. user manuals, operator manuals, etc.) supporting sustaining activities.
- Develops and delivers medical/clinical input into relevant medical device training documents (e.g. training decks, in-service scripts, e-learning tools, etc.) supporting sustaining activities.
- Contributes to development and review of risk documentation.
- Participates in development of claims matrix, identification in gaps and development of evidence generation plan in collaboration with Clinical, R&D, Marketing, and Medical Affairs Organizations
- Supports other miscellaneous projects, based on skill sets and credentials, as needed.
- Develops and maintains knowledge base for related Baxter Care Communication products.
- Provides Medical SME support for relevant EU MDD/MDR clinical and post-market surveillance deliverables (as appropriate for products in Front Line Care portfolio)
KEY QUALIFICATIONS:
- Strong problem solving and resolution skills with ability to influence and effectively work with cross-functional teams
- Sound scientific clinical approach to medical writing based on previous experience, technical writing, and ability to analyze information fostering clinical credibility
- Advanced interpersonal and communication skills with demonstrated ability to manage conflict situations
- Self-motivated with exceptional follow through, effective time management skills, and ability to multitask
- Ability to analyze, organize, and react to diverse activities in a changing environment often with time constraints
- Ability to work collaboratively and inclusively across diverse cultures
- Effective and competent presentation and educating skills
- Product development and lifecycle management experience preferred
EDUCATION & EXPERIENCES:
- Degree in nursing, nursing informatics, or other clinical discipline with relevant experience in product portfolio required
- Advanced degree preferred
- 5 years of acute adult primary care, medical surgical, or related clinical experience required; industry experience strongly preferred
- Active license within territory in good standing required with clinical expertise
OTHER REQUIREMENTS:
- Travel required domestic and internationally up to 20%
- Located in Malta
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
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